Variant report

Variant	rs61625565
Chromosome Location	chr8:105525706-105525707
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:105524828..105527045-chr8:105784519..105787055,2	K562	blood:
2	chr8:105523437..105529379-chr8:105769112..105773532,5	K562	blood:
3	chr8:105525658..105529400-chr8:105771015..105773532,3	K562	blood:
4	chr8:105523372..105526382-chr8:105598970..105602701,4	K562	blood:
5	chr8:105524457..105526235-chr8:105771233..105774016,35	MCF-7	breast:
6	chr8:105524499..105526205-chr8:105690324..105691789,15	MCF-7	breast:
7	chr8:105524219..105529091-chr8:105598970..105603591,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000253350	Chromatin interaction
ENSG00000147650	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs57142502	0.81[AFR][1000 genomes]
rs57345526	1.00[AMR][1000 genomes]
rs57576798	1.00[AMR][1000 genomes]
rs58114675	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58146190	0.81[AFR][1000 genomes]
rs59216364	1.00[AMR][1000 genomes]
rs59493567	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59637616	0.81[AFR][1000 genomes]
rs60373042	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60973921	1.00[AMR][1000 genomes]
rs61420349	1.00[AMR][1000 genomes]
rs73293273	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293281	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293282	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73293285	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73295106	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73295110	1.00[AFR][1000 genomes]
rs73295123	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73295125	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73295147	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73295152	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73295161	1.00[AMR][1000 genomes]
rs73295165	1.00[AMR][1000 genomes]
rs73295177	1.00[AMR][1000 genomes]
rs73295179	1.00[AMR][1000 genomes]
rs73295180	1.00[AMR][1000 genomes]
rs73295190	1.00[AMR][1000 genomes]
rs73297119	1.00[AMR][1000 genomes]
rs73297125	1.00[AMR][1000 genomes]
rs73297141	1.00[AMR][1000 genomes]
rs73297156	1.00[AMR][1000 genomes]
rs73297196	1.00[AMR][1000 genomes]
rs73299147	1.00[AMR][1000 genomes]
rs73299148	1.00[AMR][1000 genomes]
rs971106	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016087	chr8:105228670-105934368	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1026754	chr8:105382508-106030916	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
3	nsv539709	chr8:105382508-106030916	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	nsv831417	chr8:105455814-105625608	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:105495600-105525800	Weak transcription	Psoas Muscle	Psoas
2	chr8:105499200-105542200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:105503600-105525800	Weak transcription	HUVEC	blood vessel
4	chr8:105503800-105535800	Weak transcription	NHDF-Ad	bronchial
5	chr8:105509600-105535800	Weak transcription	Aorta	Aorta
6	chr8:105510200-105546200	Weak transcription	HMEC	breast
7	chr8:105510400-105539400	Weak transcription	HSMMtube	muscle
8	chr8:105510800-105531000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr8:105511000-105525800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr8:105511000-105527200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr8:105511000-105529800	Weak transcription	Fetal Lung	lung
12	chr8:105511800-105527000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:105511800-105532600	Weak transcription	HSMM	muscle
14	chr8:105511800-105550200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr8:105512800-105542000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr8:105512800-105550200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:105514800-105529200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr8:105515200-105542400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr8:105517600-105527000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr8:105519800-105534400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:105520200-105528400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr8:105520400-105534800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:105520600-105537400	Weak transcription	NH-A	brain
24	chr8:105520800-105536600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr8:105521000-105540000	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr8:105521400-105540000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:105521800-105568800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:105525200-105525800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:105525200-105526400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr8:105525200-105526800	Enhancers	Fetal Thymus	thymus
31	chr8:105525200-105527200	Enhancers	Primary hematopoietic stem cells	blood
32	chr8:105525200-105527400	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr8:105525200-105527400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr8:105525200-105527400	Enhancers	K562	blood
35	chr8:105525200-105528000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:105525200-105528600	Enhancers	Dnd41	blood
37	chr8:105525400-105527000	Weak transcription	Osteobl	bone
38	chr8:105525400-105527400	Enhancers	Primary T cells from cord blood	blood
39	chr8:105525400-105531200	Weak transcription	Brain Anterior Caudate	brain
40	chr8:105525600-105525800	Enhancers	Left Ventricle	heart
41	chr8:105525600-105526000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr8:105525600-105526000	Enhancers	GM12878-XiMat	blood
43	chr8:105525600-105526400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr8:105525600-105526400	Enhancers	Thymus	Thymus
45	chr8:105525600-105527200	Weak transcription	Muscle Satellite Cultured Cells	--

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